| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:93453534-93453690 | Rare:36 | ||||
| chr9:95875459-95875698 | Common:1; Rare:79 | ||||
| chr9:95875982-95876047 | Common:4; Rare:29 | ||||
| chr9:96778033-96778165 | Rare:40 | ||||
| chr9:97013587-97013836 | Common:4; Rare:69 | ||||
| chr9:97633245-97633889 | Common:6; Rare:194 | ||||
| chr9:97853124-97853231 | Rare:34 | ||||
| chr9:99221898-99222349 | Common:2; Rare:176; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:100098953-100099307 | Common:3; Rare:100; Clinvar:1 | ||||
| chr9:100352851-100353085 | Rare:85 | ||||
| chr9:101398594-101398918 | Common:1; Rare:103 | ||||
| chr9:104747583-104747802 | Common:1; Rare:67 | ||||
| chr9:105447955-105448172 | Common:2; Rare:80 | ||||
| chr9:105558016-105558184 | Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:107489764-107490057 | Common:4; Rare:126 |